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. 2005 Jun;187(12):3941–3949. doi: 10.1128/JB.187.12.3941-3949.2005

TABLE 1.

Strains and plasmids used in this study

Strain or plasmid Relevant characteristic(s)a Source or reference
Strains
    B. pertussis
        BC39 Wild type; TOHAMA III background; Nalr Smr 9, 10
        RGK343 BC39 dsbB::pRGK340; Nalr Smr Kanr This study
        Tn5 mutants See Table 2 This study
    E. coli
        S17-1 λ pir conjugation mobilizing strain Laboratory collection
        TB1 General cloning vector Laboratory collection
        CC118 Pho strain 30
        Tuner (DE3) T7 expression host Novagen
Plasmids
    pET2-Blue T7 expression vector Novagen
    pTGN Mini-Tn5gfp-km transposon; Kanr 58
    pss2141 Suicide vector for homologous recombination; Gmr Sms 56
    pUC119 Cloning vector; Ampr Laboratory collection
    pUC4-KIXX Aminoglycoside phosphotransferase Kanr cassette Pharmacia
    pRGK309 CcsB:PhoA expression vector; Tetr 3
    pRGK338 puc119-DsbB; 2,469-bp PCR product including dsbB ORF as HinDIII fragment in puc119; Ampr This study
    pRGK339 dsbB::Kanr; pRGK338 with Kanr cassette from pUC4-KIXX replacing dsbB ORF; Ampr Kanr This study
    pRGK340 dsbB::Kanr HinDIII fragment from pRGK339 in pss2141; Gmr Kanr Sms This study
    pRGK341 ccsB gene cloned into pET2-Blue with C-terminal 6 × His tag; Ampr This study
    pRGK342 CcsA replacing PhoA from pRGK309; Tetr This study
a

ORF, open reading frame.